Does BORTEZOMIB Cause Hypofibrinogenaemia? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hypofibrinogenaemia have been filed in association with BORTEZOMIB (bortezomib). This represents 0.0% of all adverse event reports for BORTEZOMIB.
8
Reports of Hypofibrinogenaemia with BORTEZOMIB
0.0%
of all BORTEZOMIB reports
6
Deaths
5
Hospitalizations
How Dangerous Is Hypofibrinogenaemia From BORTEZOMIB?
Of the 8 reports, 6 (75.0%) resulted in death, 5 (62.5%) required hospitalization, and 5 (62.5%) were considered life-threatening.
Is Hypofibrinogenaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BORTEZOMIB. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does BORTEZOMIB Cause?
Plasma cell myeloma (6,683)
Off label use (4,754)
Neuropathy peripheral (4,067)
Drug ineffective (2,730)
Diarrhoea (2,244)
Thrombocytopenia (2,082)
Death (2,025)
Pneumonia (2,020)
Fatigue (1,757)
Neutropenia (1,530)
What Other Drugs Cause Hypofibrinogenaemia?
METHOTREXATE (297)
PEGASPARGASE (296)
VINCRISTINE (295)
DAUNORUBICIN (186)
CYTARABINE (177)
DEXAMETHASONE (174)
HYDROCORTISONE (126)
PREDNISONE (124)
TOCILIZUMAB (121)
PREDNISOLONE (117)
Which BORTEZOMIB Alternatives Have Lower Hypofibrinogenaemia Risk?
BORTEZOMIB vs BOSENTAN
BORTEZOMIB vs BOSENTAN\BOSENTAN
BORTEZOMIB vs BOSULIF
BORTEZOMIB vs BOSUTINIB
BORTEZOMIB vs BOTOX